We are building the future of PTSD. Our small team values curiosity, ownership, and impact. If you want to shape a product from the ground up, we would love to hear from you
Job Listing
JOB PURPOSE & RESPONSIBILITIES
The Embedded Electronics Engineer participates in the design, development, testing and industrialization of an active implantable medical device. He/she works in a highly hands-on manner within a small, experienced and multidisciplinary team, contributing mainly to electronics and embedded software development, while interacting closely with external subcontractors and test laboratories. He/she contributes to the development of a meaningful medical product in a highly regulated environment and within a small team of passionate people.
MAIN ACTIVITIES
• Contribute to the design and development of electronic circuits (analog, digital, power electronics) for an implantable medical device, including schematic design, electronics prototyping, testing, debugging and validation activities.
• Develop embedded firmware for microcontrollers, mostly barebone, application code and associated tests.
Experience with IEC 62304-compliant development is a strong plus.
• Design and implement dedicated test devices and test benches to verify product functionalities as well as selected regulatory tests, in accordance with applicable standards such as ISO 14708-1 and IEC 60601-1.
• Participate in the development of wireless power transfer solutions for implantable systems; relevant experience and/or with electromagnetic simulation tools is considered an asset.
• Develop, maintain and improve laboratory test setups, tools and equipment used for electronics, firmware and system-level testing.
• Manage and coordinate electronic subcontractors (PCB manufacturing, assembly, test laboratories), including, but not limited to, technical follow-up, reviews and support during development and industrialization phases, with practice of design-for-manufacturing (DFM) and design-for-test (DFT) considerations throughout the product development lifecycle.
• Collaborate closely with other disciplines (mechanical design, software, quality, medical, clinical, regulatory affairs) in a fundamentally multidisciplinary environment.
• Participate in technical documentation activities related to electronics and embedded software (design documentation, test protocols, reports), supporting the Design Control Process and Design History File (DHF) when required.
HARD SKILLS
• Strong hands-on expertise in electronic design and embedded systems development.
• Solid experience in embedded software development on microcontrollers (C / C++), including debugging and testing.
• Experience with electronics testing, laboratory equipment and test setup development.
• Knowledge of manufacturing processes for electronic assemblies and experience working with electronic manufacturing subcontractors.
• Understanding of design-for-manufacturing principles.
• Ability to work autonomously within a small team of experienced and passionate engineers.
• Previous experience in supporting animal studies would be a plus.
• Knowledge of medical device regulatory standards is an asset, particularly ISO 14708-1, IEC 60601-1 and IEC 62304, as well as FDA & MDR regulations.
• Fluent written English is mandatory; spoken English is strongly preferred. Daily work environment is French-speaking.
• Willingness to travel abroad for short business trips when required.
EDUCATION REQUIREMENTS
• Master’s degree in Electronics Engineering, Embedded Systems, or equivalent.
SOFT SKILLS
• Hands-on, pragmatic and solution-oriented mindset.
• Strong autonomy and sense of responsibility.
• Excellent analytical and problem-solving skills.
• Strong collaboration and communication skills within multidisciplinary teams.
• Curiosity, adaptability and willingness to work in an innovative medical environment.
OUR OFFER
• Full-time open-ended contract and good salary package
• A friendly, dynamic and ever evolving start-up atmosphere and team
• The chance to get involved in the company evolution and in the full chain of development, from specifications to clinical investigations and market and, ultimately, help improve people’s life.
• Company location is currently in Lasne but will change soon, likely within the Brabant wallon area.
HOW TO APPLY ?
To apply please send your CV with a mandatory covering letter by e-mail to pascal.doguet@stimalia.com and olivier.menage@stimalia.com. Applications with "one click", no covering letter or indicating minimal discovery of our company was not performed will not be considered. For more information, contact us or visit our website at stimalia.com